Toasted Vanilla Sugar Hand Sanitizer

TOASTED VANILLA SUGAR HAND SANITIZER BODYCOLOGY- ethyl alcohol liquid
Advanced Beauty Systems, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient purpose

Ethyl Alcohol 75% Antiseptic

Uses: to decrease bacteria on the skin.

Keep out of reach of children.

Stop use and consult a doctor if irritation and redness develop and persist for more than 72 hours.

Warnings: For external use only.
Flammable. Keep away from heat and flame.
When using this product: Avoid contact with eyes. If contact occurs, flush eyes with water. Avoid contact with broken skin.
In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions: Wet hands with product.

Briskly rub hands together until dry.

For children under 6, use only under adult supervision.

Not recommended for infants.

Inactive ingredients: Water (aqua, eau), fragrance (parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer
triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI77007)
May contain: FD C Red No.4(CI 14700), FD C Yellow No. 5 (CI 19140), FD C Blue No.1 (CI 42090), D C Red No 33(CI 17200)

Bodycology

Moisturizing

Hand Sanitizer

with Aloe Vera

kills 99% of germs without water

Toasted Vanilla Sugar

30 mL 1 Fl Oz

TOASTED VANILLA SUGAR HAND SANITIZER BODYCOLOGY
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51345-105
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	22.5 mL in 30 mL

Ingredient Name	Strength
Inactive Ingredients
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
GELATIN (UNII: 2G86QN327L)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

#	Item Code	Package Description
Packaging
1	NDC:51345-105-01	1 in 1 BLISTER PACK
1		30 mL in 1 BOTTLE

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	04/07/2011

Labeler - Advanced Beauty Systems, Inc. (129986613)

Registrant - Advanced Beauty Systems, Inc. (129986613)

Name	Address	ID/FEI	Business Operations
Establishment
Landy International		545291775	manufacture(51345-105)